Pfizer Oncology Pipeline Takes Hit With Dacomitinib Lung Failure

Expectations for the asset hadn’t been high, but failure of two Phase III lung cancer studies of the irreversible pan-HER inhibitor dacomitinib may remove a potential competitor for Boehringer Ingelheim’s recently approved irreversible EGFR inhibitor Gilotrif.

Pfizer Inc.played a sound strategy testing its pan-HER inhibitor dacomitinib in non-small cell lung cancer – including studying it against market-leading Tarceva – but the failure of two Phase III trials are still a blow for Pfizer’s oncology pipeline.

More from Clinical Trials

More from R&D

Aragen’s CEO Says NIH Funding Cut Means Less R&D Money, And Tariffs Would Add To Woes

 
• By 

Aragen’s CEO Manni Kantipudi, who is keenly watching the Trump Administration’s moves on pharma tariffs, discusses funding cuts at the National Institutes of Health, big pharma’s US onshoring moves, and talks with the Indian government to solve intellectual property challenges in an interview.

‘Come Early, Come Often,’ EMA Chief Tells Industry

 

The European Medicines Agency’s chief, Emer Cooke, explained how the agency could help companies with their drug development plans, and said the EU Health Technology Assessment Regulation would help companies design clinical trials that are fit for regulators and HTA bodies.

Why Successful Companies Are ‘Tough On Themselves’ When It Comes To HTA

 

Pharmaceutical companies need to “pressure test” their clinical development strategies early for health technology assessment purposes, particularly in light of the new EU HTA Regulation, a life sciences consultant says.